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    Nanoplasmonic electron acceleration in silver clusters studied by angular-resolved electron spectroscopy
    (Bristol : IOP, 2012) Passig, J.; Irsig, R.; Truong, N.X.; Fennel, T.; Tiggesbäumker, J.; Meiwes-Broer, K.H.
    The nanoplasmonic field enhancement effects in the energetic electron emission from few-nm-sized silver clusters exposed to intense femtosecond dual pulses are investigated by high-resolution double differential electron spectroscopy. For moderate laser intensities of 10 14Wcm -2, the delaydependent and angular-resolved electron spectra show laser-aligned emission of electrons up to keV kinetic energies, exceeding the ponderomotive potential by two orders of magnitude. The importance of the nanoplasmonic field enhancement due to resonant Mie-plasmon excitation observed for optimal pulse delays is investigated by a direct comparison with molecular dynamics results. The excellent agreement of the key signatures in the delay-dependent and angular-resolved spectra with simulation results allows for a quantitative analysis of the laser and plasmonic contributions to the acceleration process. The extracted field enhancement at resonance verifies the dominance of surfaceplasmon-assisted re-scattering.
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    Attosecond electron spectroscopy using a novel interferometric pump-probe technique
    (College Park, Md. : APS, 2010) Mauritsson, J.; Remetter, T.; Swoboda, M.; Klünder, K.; L'Huillier, A.; Schafer, K.J.; Ghafur, O.; Kelkensberg, F.; Siu, W.; Johnsson, P.; Vrakking, M.J.J.; Znakovskaya, I.; Uphues, T.; Zherebtsov, S.; Kling, M.F.; Lépine, F.; Benedetti, E.; Ferrari, F.; Sansone, G.; Nisoli, M.
    We present an interferometric pump-probe technique for the characterization of attosecond electron wave packets (WPs) that uses a free WP as a reference to measure a bound WP. We demonstrate our method by exciting helium atoms using an attosecond pulse (AP) with a bandwidth centered near the ionization threshold, thus creating both a bound and a free WP simultaneously. After a variable delay, the bound WP is ionized by a few-cycle infrared laser precisely synchronized to the original AP. By measuring the delay-dependent photoelectron spectrum we obtain an interferogram that contains both quantum beats as well as multipath interference. Analysis of the interferogram allows us to determine the bound WP components with a spectral resolution much better than the inverse of the AP duration. © 2010 The American Physical Society.